Chen Hexun, Song Xiaochong, Huang Xiaojia
Fujian Key Laboratory of Coastal Pollution Prevention and Control, College of the Environment and Ecology, Xiamen University, Xiamen, 361005, P. R. China.
J Sep Sci. 2021 Sep;44(18):3418-3428. doi: 10.1002/jssc.202100473. Epub 2021 Jul 31.
Magnetism-assisted in-tube solid phase microextraction based on porous monolith mingled with Fe O nanoparticles was developed for capture of phenolic acids in fruit juices. First, poly (1-allyl-3-methylimidazolium bis [(trifluoro methyl) sulfonyl] imide-co-ethylene dimethacrylate) monolith embedded with Fe O nanoparticles was facile fabrication in a capillary and employed as microextraction column. Subsequently, a magnetic coil adopted to produce variable magnetic fields during extraction stage was twined on the microextraction column. The analytes contents in eluant were quantified by high performance liquid chromatogram with diode array detector. Various parameters affecting the extraction performance were inspected and optimized in detail. Results revealed that the exertion of magnetic fields in adsorption and desorption steps enhanced the extraction efficiencies of analytes from 44.9-64.0% to 78.6-87.1%. Under the optimal extraction factors, the limits of detection were between 0.012 and 0.061 μg/L, relative standard deviations for precision in terms of intra- and inter-day assay variability ranged from 1.9 to 9.8%. The introduced approach was successfully applied to simultaneously quantify the contents of five analytes in real fruit juices with satisfying fortified recoveries (80.1-116%). The obtained results well demonstrate the promising potential of the developed method in the highly sensitive quantification of trace phenolic acids in complex samples.
基于与Fe₃O₄纳米颗粒混合的多孔整体柱的磁性辅助管内固相微萃取技术被开发用于捕获果汁中的酚酸。首先,将嵌入Fe₃O₄纳米颗粒的聚(1-烯丙基-3-甲基咪唑双[(三氟甲基)磺酰]亚胺-共-二甲基丙烯酸乙烯酯)整体柱在毛细管中简便制备,并用作微萃取柱。随后,在微萃取柱上缠绕一个磁线圈,以便在萃取阶段产生可变磁场。用配备二极管阵列检测器的高效液相色谱法定量洗脱液中分析物的含量。详细考察并优化了影响萃取性能的各种参数。结果表明,在吸附和解吸步骤中施加磁场可将分析物的萃取效率从44.9-64.0%提高到78.6-87.1%。在最佳萃取条件下,检测限在0.012至0.061 μg/L之间,日内和日间精密度的相对标准偏差在1.9%至9.8%之间。所介绍的方法成功应用于同时定量实际果汁中五种分析物的含量,加标回收率令人满意(80.1-116%)。所得结果充分证明了所开发方法在复杂样品中痕量酚酸高灵敏度定量方面的潜在应用前景。